HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003821_47003822insGTA , CM000681.2:g.47003821_47003822insGTA | GRCh38 |
NC_000019.9:g.47507078_47507079insGTA , CM000681.1:g.47507078_47507079insGTA | GRCh37 |
NC_000019.8:g.52198918_52198919insGTA | NCBI36 |
NG_047014.1:g.90255_90256insGTA | |
NG_047014.2:g.147825_147826insGTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7633_7634insGTA | ENSP00000385720.2:n.7633_7634insGTA | |
ENST00000672722.1:c.*3133_*3134insGTA MANE Select | ENSP00000500409.1:n.*3133_*3134insGTA | |
ENST00000404338.7:c.7633_7634insGTA | ENSP00000385720.2:n.7633_7634insGTA | |
ENST00000614079.1:c.7210_7211insGTA | ENSP00000483730.1:n.7210_7211insGTA | |
NM_004491.4:c.7633_7634insGTA | NP_004482.4:n.7633_7634insGTA | |
NM_004491.5:c.*3133_*3134insGTA MANE Select | NP_004482.4:n.*3133_*3134insGTA |